Automated Anatomical Labeling of Activations in SPM Using a Macroscopic Anatomical Parcellation of the MNI MRI Single-Subject Brain

We review evidence for partially segregated networks of brain areas that carry out different attentional functions. One system, which includes parts of the intraparietal cortex and superior frontal cortex, is involved in preparing and applying goal-directed (top-down) selection for stimuli and responses. This system is also modulated by the detection of stimuli. The other system, which includes the temporoparietal cortex and inferior frontal cortex, and is largely lateralized to the right hemisphere, is not involved in top-down selection. Instead, this system is specialized for the detection of behaviourally relevant stimuli, particularly when they are salient or unexpected. This ventral frontoparietal network works as a 'circuit breaker' for the dorsal system, directing attention to salient events. Both attentional systems interact during normal vision, and both are disrupted in unilateral spatial neglect.

Control of goal-directed and stimulus-driven attention in the brain

▪ Abstract The prefrontal cortex has long been suspected to play an important role in cognitive control, in the ability to orchestrate thought and action in accordance with internal goals. Its neural basis, however, has remained a mystery. Here, we propose that cognitive control stems from the active maintenance of patterns of activity in the prefrontal cortex that represent goals and the means to achieve them. They provide bias signals to other brain structures whose net effect is to guide the flow of activity along neural pathways that establish the proper mappings between inputs, internal states, and outputs needed to perform a given task. We review neurophysiological, neurobiological, neuroimaging, and computational studies that support this theory and discuss its implications as well as further issues to be addressed

/pdf/an-integrative-theory-of-prefrontal-cortex-function-2j9unprn5f.pdf

An integrative theory of prefrontal cortex function

Publisher Summary This chapter focuses on the modern notion of short-term memory, called working memory. Working memory refers to the temporary maintenance of information that was just experienced or just retrieved from long-term memory but no longer exists in the external environment. These internal representations are short-lived, but can be maintained for longer periods of time through active rehearsal strategies, and can be subjected to various operations that manipulate the information in such a way that makes it useful for goal-directed behavior. Working memory is a system that is critically important in cognition and seems necessary in the course of performing many other cognitive functions, such as reasoning, language comprehension, planning, and spatial processing. This chapter demonstrates the functional importance of dopamine to working memory function in several ways. Elucidation of the cognitive and neural mechanisms underlying human working memory is an important focus of cognitive neuroscience and neurology for much of the past decade. One conclusion that arises from research is that working memory, a faculty that enables temporary storage and manipulation of information in the service of behavioral goals, can be viewed as neither a unitary, nor a dedicated system. Data from numerous neuropsychological and neurophysiological studies in animals and humans demonstrates that a network of brain regions, including the prefrontal cortex, is critical for the active maintenance of internal representations.

Chapter 11 Working memory

Recent developments in the quantitative analysis of complex networks, based largely on graph theory, have been rapidly translated to studies of brain network organization. The brain's structural and functional systems have features of complex networks--such as small-world topology, highly connected hubs and modularity--both at the whole-brain scale of human neuroimaging and at a cellular scale in non-human animals. In this article, we review studies investigating complex brain networks in diverse experimental modalities (including structural and functional MRI, diffusion tensor imaging, magnetoencephalography and electroencephalography in humans) and provide an accessible introduction to the basic principles of graph theory. We also highlight some of the technical challenges and key questions to be addressed by future developments in this rapidly moving field.

Complex brain networks: graph theoretical analysis of structural and functional systems

To aid our understanding of age-related changes in brain activation during visuoperceptual processing, we designed an experiment to test the effect of task difficulty on regional cerebral blood flow (rCBF) as measured by positron emission tomography (PET). We report here the results from 10 young subjects engaged in match-to-sample tasks of progressively degraded faces. The tasks consisted of a control task, a face matching task with no stimulus degradation, and five levels of degradation: 20%, 40%, 50%, 60%, and 70%. Both performance accuracy and reaction times deteriorated significantly with increasing face degradation. There was a significant increase of rCBF in bilateral fusiform gyri during all face-matching conditions compared to the control task, and bilateral prefrontal activation during the 70% degradation condition. Linear regression analyses revealed a significant increase of rCBF in the right prefrontal cortex, and linear decreases of rCBF in the striate and fusiform cortex as face degradation increased. Performance on the 70% task was correlated positively with rCBF in right prefrontal and bilateral fusiform gyri, and negatively with left prefrontal and striate rCBF. These results show that the right prefrontal, striate, and ventral extrastriate cortex are the principal brain regions that modulate their activity as this visual discrimination task becomes more difficult. The right prefrontal increase probably represents an increasing demand on working memory or attention, whereas decreased rCBF in the striate cortex may be due to changes in the characteristics of the stimuli, or to suppression of low-level processing by one of a number of mechanisms. This experiment has implications both for the design of neuroimaging experiments, and for interpreting differences in rCBF activation between groups.

Effect of task difficulty on cerebral blood flow during perceptual matching of faces.

The inferior longitudinal fasciculus is commonly considered to be a long association fiber bundle interconnecting the occipital and temporal lobes Based on blunt dissections of human and monkey brains, we have found that the only long fiber bundle common to both the occipital and temporal lobes is the geniculostriate pathway (ie, optic radiations), located within the external sagittal stratum In addition, our autoradiographic experiments indicate that the pathway from the occipital to the temporal cortex in monkeys consists of a series of U fibers that course beneath the cortical mantle to connect adjacent regions in striate, prestriate, and inferior temporal cortex We suggest that the occipital and temporal lobes in human beings are similarly connected by a series of U fibers and that the term inferior longitudinal fasciculus be replaced with the term occipitotemporal projection system Different clinical syndromes attributed to lesions of the inferior longitudinal fasciculus, including visual agnosia, prosopagnosia, and impaired visual recent memory, are probably due to interruption of fibers at different points along this projection system

The inferior longitudinal fasciculus: A reexamination in humans and monkeys

The ability to perceive and differentiate facial expressions is vital for social communication. Numerous functional MRI (fMRI) studies in humans have shown enhanced responses to faces with different emotional valence, in both the amygdala and the visual cortex. However, relatively few studies have examined how valence influences neural responses in monkeys, thereby limiting the ability to draw comparisons across species and thus understand the underlying neural mechanisms. Here we tested the effects of macaque facial expressions on neural activation within these two regions using fMRI in three awake, behaving monkeys. Monkeys maintained central fixation while blocks of different monkey facial expressions were presented. Four different facial expressions were tested: (i) neutral, (ii) aggressive (open-mouthed threat), (iii) fearful (fear grin), and (iv) submissive (lip smack). Our results confirmed that both the amygdala and the inferior temporal cortex in monkeys are modulated by facial expressions. As in human fMRI, fearful expressions evoked the greatest response in monkeys—even though fearful expressions are physically dissimilar in humans and macaques. Furthermore, we found that valence effects were not uniformly distributed over the inferior temporal cortex. Surprisingly, these valence maps were independent of two related functional maps: (i) the map of “face-selective” regions (faces versus non-face objects) and (ii) the map of “face-responsive” regions (faces versus scrambled images). Thus, the neural mechanisms underlying face perception and valence perception appear to be distinct.

https://www.pnas.org/content/pnas/105/14/5591.full.pdf

Perception of emotional expressions is independent of face selectivity in monkey inferior temporal cortex

To determine the locus, full extent, and topographic organization of cortical connections of area V4 (visual area 4), we injected anterograde and retrograde tracers under electrophysiological guidance into 21 sites in 9 macaques. Injection sites included representations ranging from central to far peripheral eccentricities in the upper and lower fields. Our results indicated that all parts of V4 are connected with occipital areas V2 (visual area 2), V3 (visual area 3), and V3A (visual complex V3, part A), superior temporal areas V4t (V4 transition zone), MT (medial temporal area), and FST (fundus of the superior temporal sulcus [STS] area), inferior temporal areas TEO (cytoarchitectonic area TEO in posterior inferior temporal cortex) and TE (cytoarchitectonic area TE in anterior temporal cortex), and the frontal eye field (FEF). By contrast, mainly peripheral field representations of V4 are connected with occipitoparietal areas DP (dorsal prelunate area), VIP (ventral intraparietal area), LIP (lateral intraparietal area), PIP (posterior intraparietal area), parieto-occipital area, and MST (medial STS area), and parahippocampal area TF (cytoarchitectonic area TF on the parahippocampal gyrus). Based on the distribution of labeled cells and terminals, projections from V4 to V2 and V3 are feedback, those to V3A, V4t, MT, DP, VIP, PIP, and FEF are the intermediate type, and those to FST, MST, LIP, TEO, TE, and TF are feedforward. Peripheral field projections from V4 to parietal areas could provide a direct route for rapid activation of circuits serving spatial vision and spatial attention. By contrast, the predominance of central field projections from V4 to inferior temporal areas is consistent with the need for detailed form analysis for object vision.

/pdf/subcortical-connections-of-area-v4-in-the-macaque-4g5th25bi6.pdf

Subcortical connections of area V4 in the macaque

To elucidate the neural basis of the recognition of tactile form and location, we used functional MRI while subjects discriminated gratings delivered to the fingertip of either the right or left hand. Subjects were required to selectively attend to either grating orientation or grating location under identical stimulus conditions. Independent of the hand that was stimulated, grating orientation discrimination selectively activated the left intraparietal sulcus, whereas grating location discrimination selectively activated the right temporoparietal junction. Hence, hemispheric dominance appears to be an organizing principle for cortical processing of tactile form and location.

http://www.pnas.org/content/102/35/12601.full.pdf

Leslie G. Ungerleider

Papers

Effect of task difficulty on cerebral blood flow during perceptual matching of faces.

The inferior longitudinal fasciculus: A reexamination in humans and monkeys

Perception of emotional expressions is independent of face selectivity in monkey inferior temporal cortex

Subcortical connections of area V4 in the macaque

Tactile form and location processing in the human brain